Author

Triki Ch

Observed names: C H Triki, C. Charfi Triki

Institutions: University of Sfax, Hopital Universitaire Hedi Chaker, Faculty of Medicine of Sfax

Observed institutions: University of Sfax, Hopital Universitaire Hedi Chaker, Faculty of Medicine of Sfax

OpenAlex ID: A5112402818

[Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].

1991 · M Ben Hamida, N Attia-Romdhane, et al. · PubMed · 10

Novel mutations in LAMA2 gene responsible for a severe phenotype of congenital muscular dystrophy in two Tunisian families.

2006 · N Louhichi, P Richard, et al. · PubMed · 4

Caregiver burden in parents of children with neurological impairement and its relation with depression

2023 · A. Mellouli, S. Zouari, et al. · European Psychiatry · 1

Specific learning disorders and psychiatric comorbidities in school children in Sfax, Tunisia

2018 · Cherif L, Ayedi H, et al. · Trends in Medicine · 1

Works count: 5

Citation count: 16

H-index: 2

I10-index: 1